Canonical Allele Identifier: PA2827924105
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2140600
ClinVar RCV Id: RCV003542382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Phe1937Ser
CA352139634
NM_001354701.2:c.5810T>C